decreased trabecular bone volume Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description decrease in the amount of space occupied by trabecular bone tissue in the skeleton (Mammalian Phenotype Ontology, MP_0010879)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0010879
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Genes

27 gene mutations causing the decreased trabecular bone volume phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ADIPOQ adiponectin, C1Q and collagen domain containing
ANKH ANKH inorganic pyrophosphate transport regulator
CHSY1 chondroitin sulfate synthase 1
CLDN18 claudin 18
CLEC2D C-type lectin domain family 2, member D
COL2A1 collagen, type II, alpha 1
CST5 cystatin D
FAM20C family with sequence similarity 20, member C
FIG4 FIG4 phosphoinositide 5-phosphatase
FZD9 frizzled class receptor 9
GNPTAB N-acetylglucosamine-1-phosphate transferase, alpha and beta subunits
GPR65 G protein-coupled receptor 65
INPP5D inositol polyphosphate-5-phosphatase, 145kDa
IRAK3 interleukin-1 receptor-associated kinase 3
ISG15 ISG15 ubiquitin-like modifier
KITLG KIT ligand
KLF10 Kruppel-like factor 10
MCPH1 microcephalin 1
PDIA3 protein disulfide isomerase family A, member 3
POSTN periostin, osteoblast specific factor
PRDM5 PR domain containing 5
RASSF2 Ras association (RalGDS/AF-6) domain family member 2
ROR2 receptor tyrosine kinase-like orphan receptor 2
SH3BP2 SH3-domain binding protein 2
TMEM119 transmembrane protein 119
TWSG1 twisted gastrulation BMP signaling modulator 1
WWOX WW domain containing oxidoreductase